8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Liao C, Sarayloo F, Vuokila V, Rochefort D, Akçimen F, Diamond S, Houle G, Laporte AD, Spiegelman D, He Q, Catoire H, Dion PA, Rouleau GA. Transcriptomic Changes Resulting From Overexpression Identify Pathways Potentially Relevant to Essential Tremor. Frontiers in Genetics. 11: 813. PMID 32849812 DOI: 10.3389/Fgene.2020.00813  0.76
2020 Sarayloo F, Spiegelman D, Rochefort D, Akçimen F, De Barros Oliveira R, Dion PA, Rouleau GA. SKOR1 has a transcriptional regulatory role on genes involved in pathways related to restless legs syndrome. European Journal of Human Genetics : Ejhg. PMID 32572201 DOI: 10.1038/S41431-020-0670-4  0.76
2020 Liao C, Sarayloo F, Rochefort D, Houle G, Akçimen F, He Q, Laporte AD, Spiegelman D, Poewe W, Berg D, Müller S, Hopfner F, Deuschl G, Kuhlenbäeumer G, Rajput A, et al. Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 32249994 DOI: 10.1002/Mds.28031  0.76
2019 Akçimen F, Ross JP, Bourassa CV, Liao C, Rochefort D, Gama MTD, Dicaire MJ, Barsottini OG, Brais B, Pedroso JL, Dion PA, Rouleau GA. Investigation of the Repeat Expansion in a Canadian and a Brazilian Ataxia Cohort: Identification of Novel Conformations. Frontiers in Genetics. 10: 1219. PMID 31824583 DOI: 10.3389/Fgene.2019.01219  0.76
2019 Sarayloo F, Dionne-Laporte A, Catoire H, Rochefort D, Houle G, Ross JP, Akçimen F, Barros Oliveira R, Turecki G, Dion PA, Rouleau GA. Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression. Plos One. 14: e0225186. PMID 31725784 DOI: 10.1371/Journal.Pone.0225186  0.76
2019 Akçimen F, Ross JP, Sarayloo F, Liao C, De Barros Oliveira R, Ruskey JA, Bourassa CV, Dion PA, Xiong L, Gan-Or Z, Rouleau GA. Genetic and epidemiological characterization of restless legs syndrome in Québec. Sleep. PMID 31665514 DOI: 10.1093/Sleep/Zsz265  0.76
2019 Liao C, Laporte AD, Spiegelman D, Akçimen F, Joober R, Dion PA, Rouleau GA. Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes. Nature Communications. 10: 4450. PMID 31575856 DOI: 10.1038/S41467-019-12450-9  0.76
2018 Akçimen F, Spiegelman D, Dionne-Laporte A, Gan-Or Z, Dion PA, Rouleau GA. Screening of novel restless legs syndrome-associated genes in French-Canadian families. Neurology. Genetics. 4: e296. PMID 30637332 DOI: 10.1212/Nxg.0000000000000296  0.76
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